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When Long Noncoding RNAs Meet Genome Editing in Pluripotent Stem Cells
Most of the human genome can be transcribed into RNAs, but only a minority of these regions produce protein-coding mRNAs whereas the remaining regions are transcribed into noncoding RNAs. Long noncoding RNAs (lncRNAs) were known for their influential regulatory roles in multiple biological processes...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5733163/ https://www.ncbi.nlm.nih.gov/pubmed/29333164 http://dx.doi.org/10.1155/2017/3250624 |
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author | Chen, Fuquan Ji, Jiaojiao Shen, Jian Lu, Xinyi |
author_facet | Chen, Fuquan Ji, Jiaojiao Shen, Jian Lu, Xinyi |
author_sort | Chen, Fuquan |
collection | PubMed |
description | Most of the human genome can be transcribed into RNAs, but only a minority of these regions produce protein-coding mRNAs whereas the remaining regions are transcribed into noncoding RNAs. Long noncoding RNAs (lncRNAs) were known for their influential regulatory roles in multiple biological processes such as imprinting, dosage compensation, transcriptional regulation, and splicing. The physiological functions of protein-coding genes have been extensively characterized through genome editing in pluripotent stem cells (PSCs) in the past 30 years; however, the study of lncRNAs with genome editing technologies only came into attentions in recent years. Here, we summarize recent advancements in dissecting the roles of lncRNAs with genome editing technologies in PSCs and highlight potential genome editing tools useful for examining the functions of lncRNAs in PSCs. |
format | Online Article Text |
id | pubmed-5733163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-57331632018-01-14 When Long Noncoding RNAs Meet Genome Editing in Pluripotent Stem Cells Chen, Fuquan Ji, Jiaojiao Shen, Jian Lu, Xinyi Stem Cells Int Review Article Most of the human genome can be transcribed into RNAs, but only a minority of these regions produce protein-coding mRNAs whereas the remaining regions are transcribed into noncoding RNAs. Long noncoding RNAs (lncRNAs) were known for their influential regulatory roles in multiple biological processes such as imprinting, dosage compensation, transcriptional regulation, and splicing. The physiological functions of protein-coding genes have been extensively characterized through genome editing in pluripotent stem cells (PSCs) in the past 30 years; however, the study of lncRNAs with genome editing technologies only came into attentions in recent years. Here, we summarize recent advancements in dissecting the roles of lncRNAs with genome editing technologies in PSCs and highlight potential genome editing tools useful for examining the functions of lncRNAs in PSCs. Hindawi 2017 2017-11-23 /pmc/articles/PMC5733163/ /pubmed/29333164 http://dx.doi.org/10.1155/2017/3250624 Text en Copyright © 2017 Fuquan Chen et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Chen, Fuquan Ji, Jiaojiao Shen, Jian Lu, Xinyi When Long Noncoding RNAs Meet Genome Editing in Pluripotent Stem Cells |
title | When Long Noncoding RNAs Meet Genome Editing in Pluripotent Stem Cells |
title_full | When Long Noncoding RNAs Meet Genome Editing in Pluripotent Stem Cells |
title_fullStr | When Long Noncoding RNAs Meet Genome Editing in Pluripotent Stem Cells |
title_full_unstemmed | When Long Noncoding RNAs Meet Genome Editing in Pluripotent Stem Cells |
title_short | When Long Noncoding RNAs Meet Genome Editing in Pluripotent Stem Cells |
title_sort | when long noncoding rnas meet genome editing in pluripotent stem cells |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5733163/ https://www.ncbi.nlm.nih.gov/pubmed/29333164 http://dx.doi.org/10.1155/2017/3250624 |
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